Canonical Allele Identifier: CA1941477234
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506797G= , CM000672.2:g.122506797G= GRCh38
NC_000010.10:g.124266313G= , CM000672.1:g.124266313G= GRCh37
NC_000010.9:g.124256303G= NCBI36
NG_011554.1:g.50273G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.884G= MANE Select ENSP00000357980.3:p.Gly295=
ENST00000648167.1:c.566G= ENSP00000498033.1:p.Gly189=
ENST00000368984.7:c.884G= ENSP00000357980.3:p.Gly295=
ENST00000420892.1:c.107G= ENSP00000412676.1:p.Gly36=
NM_002775.4:c.884G= NP_002766.1:p.Gly295=
NM_002775.5:c.884G= MANE Select NP_002766.1:p.Gly295=